The degradation of TYR variants derived from Chinese OCA families is mediated by the ERAD and ERLAD pathway
Article in Gene (August 2024)
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Identifying genetic defects in oculocutaneous albinism patients of West Bengal, Eastern India
Article in Molecular Biology Reports (July 2024)
TYR mutation in a Chinese population with oculocutaneous albinism: Molecular characteristics and ophthalmic manifestations
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